NDC 50090-5163 – Bupropion Hydrochloride

Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50090-5163

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210497
Marketed since
November 8, 2018
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for bupropion hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
50090-5163-090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-0)Sep 23, 2020
50090-5163-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-1)Sep 23, 2020
50090-5163-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5163-2)Sep 23, 2020

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